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Concord, Ohio Full Time Posted: Wednesday, 17 October 2018
 
 
Applicants who require a work visa considered

Essential Responsibilities

  • Develop and validate stability-indicating HPLC procedures for small molecule drug substances and drug products.
  • Perform forced degradation studies and develop stability indicating assay and impurities methods
  • Work in a GMP laboratory. Coordinate the timely and compliant generation of data to support client projects.
  • Perform routine HPLC analysis and validation studies
  • Author protocols and reports. Review data for technical content and regulatory compliance.
  • Maintain current expertise with relevant ICH, GMP, and FDA guidelines.

Requirements Educational Qualifications

B.S. to Ph.D. in chemistry or related field with 5+ years analytical laboratory experience or equivalent combination of education and experience is required. Relevant experience in good manufacturing practices (GMP) laboratory is required.

Specific Skills and Requirements

  • Experience in standard lab instrumentation (HPLC, UPLC, etc.)
  • Experience with LCMS or GC preferred but not required
  • Be proficient in LIMS, Microsoft Excel, and Word
  • Must have basic knowledge chemicals their properties, structure, reactivity, and be able to handle with safe and appropriate techniques.
  • Must have basic knowledge of arithmetic, algebra, and statistics.
  • Must be able to communicate effectively with all plant and office personnel.
  • Must be able to effectively multi-task

Olon Ricerca Bioscience LLC. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.


Concord, Ohio, United States of America
Science
Human Resources
CB
10/17/2018 8:01:42 AM

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